FDA UDI In Commercial Distribution 🇺🇸 United States

Canaveral®

DI: B183117950700 · Model: Canaveral® · FLOSPINE LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Canaveral®
Primary DI
B183117950700
Version / Model
Canaveral®
Catalog Number
01-1355-70
Company Name
FLOSPINE LLC
Labeler DUNS
042993143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
85e1d781-628f-483a-bf11-f379d60e9ee6

Device Description

Closed Screw Assembly, 9.5mm x 70mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
KWP Appliance, Fixation, Spinal Interlaminal
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary B183117950700

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K141850 000